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(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one is a compound belonging to the thiazolidin-4-one class, characterized by a thiazolidin-4-one ring with benzylidene and phenylimino substituents. It possesses potential biological and pharmacological activities, such as anti-inflammatory, anti-cancer, anti-bacterial, and anti-fungal properties.
Used in Pharmaceutical Industry:
(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one is used as a starting material in organic synthesis for the preparation of various pharmaceutical agents and biologically active compounds. Its structural and chemical properties make it a versatile and important molecule in medicinal and pharmaceutical research.
Used in Anti-inflammatory Applications:
(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one is used as an anti-inflammatory agent, potentially providing relief from inflammation and related symptoms.
Used in Anti-cancer Applications:
(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one is used as an anti-cancer agent, potentially contributing to the development of new cancer treatments.
Used in Anti-bacterial Applications:
(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one is used as an anti-bacterial agent, potentially aiding in the development of new antibiotics.
Used in Anti-fungal Applications:
(2Z)-5-benzylidene-3-phenyl-2-(phenylimino)-1,3-thiazolidin-4-one is used as an anti-fungal agent, potentially contributing to the development of new anti-fungal medications.

803-67-8

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803-67-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 803-67-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 803-67:
(5*8)+(4*0)+(3*3)+(2*6)+(1*7)=68
68 % 10 = 8
So 803-67-8 is a valid CAS Registry Number.

803-67-8Relevant academic research and scientific papers

Synthesis, crystal structure and biological evaluation of 5-arylidine derivatives of 3-phenyl-2-(phenylimino)thiazolidin-4-one

Haroon, Muhammad,Akhtar, Tashfeen,Tahir, Muhammad Nawaz,Ali, Imran,Hameed, Shahid

, p. 614 - 618 (2017/11/06)

Summary: Arylidene derivatives of 3-phenyl-2-(phenylimino)thiazolidin-4-ones are prepared by its condensation with respective aromatic aldehydes. The structures of synthesized compounds are established using FTIR, 13C-NMR, 1H-NMR, mass spectrometry. The s

Synthesis and antibacterial activity of 2-{[3-phenyl-7-substituted-2- (phenylimino)-2,3-dihydro[1,3]thiazolo[4,5-d]pyrimidin-5-yl]imino} -3-ethoxyphthalimido-1,3-thiazolidin-4-one

Pemawat, Gangotri,Dangi, Raja Ram,Talesara, Ganpat L.

experimental part, p. 1351 - 1358 (2011/09/20)

In the present investigation, desired fused ring system 2-{[3-phenyl-7-substituted-2-(phenylimino)-2,3-dihydro[1,3]thiazolo[4,5-d] pyrimidin-5-yl]imino}-3-ethoxyphthalimido-1,3-thiazolidin-4-one (6a-e) have been described. N,N′-Diphenylthiourea is convert

Introduction of selenium to heterocyclic compounds. Part VI. Synthesis of 3-aryl-5-benzylidene- and 3-aryl-5-cinnamylidene-2-selenorhodanines

Tejchman,Korohoda

, p. 1124 - 1134 (2007/10/03)

Three new 3-aryl-5-benzylidene-2-selenorhodanines and seven new 3-aryl-5-cinnamylidene-2-selenorhodanines were obtained by treatment with H2Se of methylation products of appropriate 2-iminothiazolidine-4-one derivatives.

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